Have questions? Visit https://www.reddit.com/r/SNPedia

rs137854653

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854653(C;C)
Make rs137854653(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356904
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854653
ebirs137854653
HLIrs137854653
Exacrs137854653
Varsomers137854653
Maprs137854653
PheGenIrs137854653
hapmaprs137854653
1000 genomesrs137854653
hgdprs137854653
ensemblrs137854653
gopubmedrs137854653
geneviewrs137854653
scholarrs137854653
googlers137854653
pharmgkbrs137854653
gwascentralrs137854653
openSNPrs137854653
23andMers137854653
23andMe allrs137854653
SNP Nexus

SNPshotrs137854653
SNPdbers137854653
MSV3drs137854653
GWAS Ctlgrs137854653
Max Magnitude0
ClinVar
Risk rs137854653(C,T;C,T)
Alt rs137854653(C,T;C,T)
Reference rs137854653(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324681C>A; NC_000006.11:g.31324681C>G
CLNSRC
CLNACC